EP0294596B1 - Mold for slip casting - Google Patents

Mold for slip casting Download PDF

Info

Publication number
EP0294596B1
EP0294596B1 EP88107320A EP88107320A EP0294596B1 EP 0294596 B1 EP0294596 B1 EP 0294596B1 EP 88107320 A EP88107320 A EP 88107320A EP 88107320 A EP88107320 A EP 88107320A EP 0294596 B1 EP0294596 B1 EP 0294596B1
Authority
EP
European Patent Office
Prior art keywords
mold
compact
organic matter
powders
slip casting
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
EP88107320A
Other languages
German (de)
French (fr)
Other versions
EP0294596A3 (en
EP0294596A2 (en
Inventor
Hiroaki Patent & License And Quality Nishio
Takeshi Patent & License And Quality Kawashima
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
JFE Engineering Corp
Original Assignee
Nippon Kokan Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Nippon Kokan Ltd filed Critical Nippon Kokan Ltd
Publication of EP0294596A2 publication Critical patent/EP0294596A2/en
Publication of EP0294596A3 publication Critical patent/EP0294596A3/en
Application granted granted Critical
Publication of EP0294596B1 publication Critical patent/EP0294596B1/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Images

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B28WORKING CEMENT, CLAY, OR STONE
    • B28BSHAPING CLAY OR OTHER CERAMIC COMPOSITIONS; SHAPING SLAG; SHAPING MIXTURES CONTAINING CEMENTITIOUS MATERIAL, e.g. PLASTER
    • B28B1/00Producing shaped prefabricated articles from the material
    • B28B1/26Producing shaped prefabricated articles from the material by slip-casting, i.e. by casting a suspension or dispersion of the material in a liquid-absorbent or porous mould, the liquid being allowed to soak into or pass through the walls of the mould; Moulds therefor ; specially for manufacturing articles starting from a ceramic slip; Moulds therefor
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B28WORKING CEMENT, CLAY, OR STONE
    • B28BSHAPING CLAY OR OTHER CERAMIC COMPOSITIONS; SHAPING SLAG; SHAPING MIXTURES CONTAINING CEMENTITIOUS MATERIAL, e.g. PLASTER
    • B28B7/00Moulds; Cores; Mandrels
    • B28B7/34Moulds, cores, or mandrels of special material, e.g. destructible materials
    • B28B7/342Moulds, cores, or mandrels of special material, e.g. destructible materials which are at least partially destroyed, e.g. broken, molten, before demoulding; Moulding surfaces or spaces shaped by, or in, the ground, or sand or soil, whether bound or not; Cores consisting at least mainly of sand or soil, whether bound or not

Definitions

  • the present invention relates to a mold for slip casting to obtain a compact by means of casting slip.
  • the method for slip casting is roughly classified into two, depending on the way of solidifying slip.
  • One method uses a mold having a feature of absorbing liquid and comprising gypsum or porous resin, wherein a part of liquid content in slip cast into this mold is absorbed in the mold to give a feature of maintaining a shape to the slip and then to form a compact by demolding.
  • Another one uses a mold having a feature of not absorbing liquid and comprising metal, rubber or the like.
  • the mold is cooled down to the melting point temperature of the liquid contained in the slip or less in advance to cast the slip into the mold, or the slip is firstly cast into the mold at room temperature and thereafter the mold is cooled down to the melting point temperature of the liquid or less, and then, the liquid is solidified to give the feature of maintaing a shape to the slip.
  • the compact is thus prepared by demolding the mold.
  • a method of using a gypsum mold containing an organic matter insoluble in water by making use of water as a dispersion medium is disclosed.
  • This mold features lowering its own strength by absorption of moisture to break down of itself, and resultantly this method facilitates the work of demolding the mold.
  • this method has an effect, in particular, on application to a mold having a complicated shape.
  • the biggest disadvantage of this method is that this mold cannot be applied to metal powders and non-oxide ceramic powders having no affinity to water, and the coverage of the usage is so limited.
  • the object of the present invention is to provide a mold for slip casting applicable to whatever shape the mold has and still applicable not only to oxide ceramic powders but also to non-oxide powders.
  • a mold for slip casting comprising a compact which is formed out of a mixture of an organic matter and powders, the organic matter being capable of being extracted by supercritical fluid and having a melting point of 0 to 150°C and the powders being incapable of being extracted by the supercritical fluid.
  • a mold for slip casting which is formed out of an organic matter capable of being extracted by means of supercritical fluid and having a melting point of 0 to 150°C.
  • a supercritical fluid in this specification means a fluid of a critical pressure and more, and still a critical temperature and more. Because the supercritical fluid has density nearly equal to that of liquid, viscosity nearly to that of gas and diffusing power almost 100 times as large as that of liquid, the supercritical fluid can be made use of as an efficient solvent in comparison with liquid solvent. As the supercritical fluid used in the present invention, a matter having a comparatively low supercritical temperature of 0 to 150°C is preferable.
  • the supercritical fluid can be any one selected from the group consisting of ethane, ethylene, carbon dioxide, monochlorotrifluoromethane, trichloromonofluoromethane and ammonia.
  • an organic matter capable of being extracted by means of the supercritical fluid one having a meltig point of 0 to 150°C is preferable.
  • An organic matter with a melting point of less than 0°C is hard to treat, because the organic matter is easy to melt at room temperature after a mold thereof is formed.
  • an organic matter having a melting point of more than 150°C is easy to give wrinkles to the surface of a compact at the forming process, because the organic matter is required to be heated for raising the temperatue of more than 150°C in advance of slip casting.
  • an organic matter preferable to be used in the present invention is anyone selected from the group consisting of methyl carbonate, t-butyl alcohol, stearic acid, stearyl alcohol and paraffin.
  • a mixture having the above-mentioned organic matter and powders incapable of being extracted by supercritical fluid is formed into a compact, and the compact is used as a mold for slip casting.
  • the powders metal powders and ceramic powders are preferable.
  • metal powders powders of 1 to 1,000 ⁇ m in particle size having good flowability is preferable.
  • iron powders and iron alloy powders which are manufactured by means of gas atomizing method are preferable.
  • ceramic powders powders of 0.2 to 10 ⁇ m in particle size having good flowability are preferable.
  • silica and alumina can be mentioned.
  • a mixture of an organic matter and powders consists of vol. 45% or less of the powders and the rest of the organic matter.
  • the organic matter alone can be used in stead of the mixture. If the ratio of the powders is of 45wt.% or less, the mold breaks down of itself by means of extracting the organic matter supercritically. If the ratio is over 45wt.%, the mold gets hard to break down of itself. If the mixture is used, the amount of the organic matter can be decreased, compared with the case of the organic matter alone being used. So, time for extraction can be shortened. It is recommendable that the formation of the mixture or of the organic matter alone is performed by means of press forming or cast forming.
  • the mold of a compact having the organic matter and the powders incapable of being extracted by means of the supercritical fluid or the mold having exclusively the organic matter capable of being extracted by means of the supercritical fluid can be prepared by the following methods:
  • Metal powder or ceramic powder is dispersed into the liquid dispersion medium to prepare slurry, the liquid dispersion medium being water, organic solvent and paraffin.
  • the organic solvent methyl carbonate, t-butyl alcohol, methyl alcohol, ethyl alcohol, butyl alcohol, hexane and benzene are preferable. Paraffin of 40 to 80°C can be preferably used.
  • ceramic oxide such as alumina and zirconium is dispersed.
  • non-oxide ceramics such as silicon nitride, silicon carbide and aluminium nitride are dispersed.
  • the paraffin ceramic oxide and non-oxide ceramics are dispersed.
  • the slurry thus prepared is cast into the mold formed in the manner as mentioned in the above. After a part of the dispersion medium is absorbed in the mold, or the dispersion medium is solidified, separable parts constituting the mold are taken away. Parts hard to be separated constituting the mold i.e. a core of a complicated shape is formed by letting an organic matter capable of being extracted by supercritical fluid contained in the core. A compact is formed by means of slip casting, and then the compact is processed by a device for supercritical extraction, thereby the organic matter in the mold being removed and the mold being melted away or breaking down of itself.
  • a dispersion medium contained in the compact is formed out of an organic matter capable of being extracted, it is advantageous that in the process of the supercritical extraction, the removal of the dispersion medium in the compact is simultaneously performed.
  • organic matter methyl carbonate, t-butyl alcohol, methyl alcohol, ethyl alcohol, butyl alcohol, hexane and benzene can be preferably used.
  • a mold of the present invention When the mold of the present invention is used, the mold melts away or breaks down of itself. Consequently, a hollow compact requiring such a complicatedly shaped core as to fail to be drawn out of the mold can be easily used. Moreover, when a main mold is prepared in accordance with the present invention, the main mold is not required to have a divisible consitution, and resultantly, a compact with precision in demension can be obtained. Besides, a dispersion medium constituting slip is not necessarily limited to water, and therefore, non-aqueous dispersion medium can be applied to molding not only ceramic powders but also metal powders and non-oxide ceramic powers. Furthermore, if a dispersion medium in the compact is formed out of an organic matter capable of being extracted supercritically, the dispersion in the compact can be simultaneously removed.
  • Granular paraffin having a melting point of 42 to 44°C was formed by hydraulic press into core 1 of a shape of a disc with a cylinder put thereon, the size of the disc being 30mm in diameter and 10mm in thickness and the size of the cylinder being 10mm in diameter and 10mm in height.
  • Fig. 1 shows an elevatioanl view of a mold for slip casting. Core 1 was assembled together with upper metallic mold 2 having a cooling jacket divisible into two portions and lower disc-shaped metallic mold 3 having gate 4 in its center axis to form a metal mold for slip casting. It should be noted that the metal mold thus formed had an inside diameter of 60mm and an inside height of 20mm.
  • slip of cilicon nitride using, as a dispersion medium, paraffin with a melting point of 42 to 44°C contained in a composition shown in Table 1, was heated and fluidized.
  • the fluidized slip was cast into the metal mold for slip casting, which had been water-cooled, and was kept at a pressure of 3kg/cm2 for 2 minutes and a half.
  • the metal mold was demolded, and molded body 5 with core 1 attached thereto as shown in Fig. 2, was obtained. After cutting of the portion of gate 4 attached to molded body 5, the molded body was put into a device for supercritical extraction.
  • the molded body was kept at 40°C and at 300kg/cm2 for 2 hours, while carbon dioxide was passed therethrough to remove paraffin and oleic acid. Subsequently, the carbon dioxide was exhausted by two hour pressure reduction, and then, resultantly, as shown in Fig. 3, the core having disappeared and the dispersion medium having been extracted, finally molded body 6 was obtained.
  • Example-1 71wt.% alumina was added to 29wt.% granular paraffin having a melting point of 42 to 44°C to prepare a mixture.
  • the mixture was heated to 60°C to be in the state of melting and then it was stirred and mixed. Thereafter, the mixture was cast into the same metal mold as used in Example-1.
  • the metal mold was cooled and demolded to obtain a similar core to that (core 1) shown in Fig. 1, and then, the same metallic mold for slip casting as used in Example-1 was constituted.

Description

  • The present invention relates to a mold for slip casting to obtain a compact by means of casting slip.
  • The method for slip casting is roughly classified into two, depending on the way of solidifying slip. One method uses a mold having a feature of absorbing liquid and comprising gypsum or porous resin, wherein a part of liquid content in slip cast into this mold is absorbed in the mold to give a feature of maintaining a shape to the slip and then to form a compact by demolding. Another one uses a mold having a feature of not absorbing liquid and comprising metal, rubber or the like. In this method, the mold is cooled down to the melting point temperature of the liquid contained in the slip or less in advance to cast the slip into the mold, or the slip is firstly cast into the mold at room temperature and thereafter the mold is cooled down to the melting point temperature of the liquid or less, and then, the liquid is solidified to give the feature of maintaing a shape to the slip. The compact is thus prepared by demolding the mold.
  • According to those methods mentioned above, when a hollow compact having a complicated inside shape, i.e. one requiring a core being too complicated and hard in shape to be drawn out of the mold because the slope is open toward the inside, the core has to be given a drawing slope so as to make it easy to draw out the core. For this reason, contrivance such as making a core composed of divisible parts is adopted. But, some drawbacks take place, for example, a hollow shape of the core has to be limited, or assembling of the divisible parts becomes difficult. Another method is considered, wherein a core is made of gypsum, and the core is broken after the completion of a compact, but the compact is easy to crack or chip during the work of breaking the core.
  • Furthermore, in a Japanese Patent Application Laid Open No. 190811/84 a method of using a gypsum mold containing an organic matter insoluble in water by making use of water as a dispersion medium, is disclosed. This mold features lowering its own strength by absorption of moisture to break down of itself, and resultantly this method facilitates the work of demolding the mold. In this point, this method has an effect, in particular, on application to a mold having a complicated shape. The biggest disadvantage of this method is that this mold cannot be applied to metal powders and non-oxide ceramic powders having no affinity to water, and the coverage of the usage is so limited.
  • The object of the present invention is to provide a mold for slip casting applicable to whatever shape the mold has and still applicable not only to oxide ceramic powders but also to non-oxide powders.
  • To attain the object, in accordance with the present invention, a mold for slip casting is provided, comprising a compact which is formed out of a mixture of an organic matter and powders, the organic matter being capable of being extracted by supercritical fluid and having a melting point of 0 to 150°C and the powders being incapable of being extracted by the supercritical fluid.
  • Furthermore, a mold for slip casting which is formed out of an organic matter capable of being extracted by means of supercritical fluid and having a melting point of 0 to 150°C.
    • Fig. 1 is an elevational view in section showing a mold for slip casting of Example-1 according to the present invention;
    • Fig. 2 is an elevational view in section showing a molded body with a core attached thereto of Example-1; and
    • Fig. 3 is an elevational view in section showing a molded body finally produced of Example-1.
  • A supercritical fluid in this specification means a fluid of a critical pressure and more, and still a critical temperature and more. Because the supercritical fluid has density nearly equal to that of liquid, viscosity nearly to that of gas and diffusing power almost 100 times as large as that of liquid, the supercritical fluid can be made use of as an efficient solvent in comparison with liquid solvent. As the supercritical fluid used in the present invention, a matter having a comparatively low supercritical temperature of 0 to 150°C is preferable. The supercritical fluid can be any one selected from the group consisting of ethane, ethylene, carbon dioxide, monochlorotrifluoromethane, trichloromonofluoromethane and ammonia.
  • As an organic matter capable of being extracted by means of the supercritical fluid, one having a meltig point of 0 to 150°C is preferable. An organic matter with a melting point of less than 0°C is hard to treat, because the organic matter is easy to melt at room temperature after a mold thereof is formed. On the other hand, an organic matter having a melting point of more than 150°C is easy to give wrinkles to the surface of a compact at the forming process, because the organic matter is required to be heated for raising the temperatue of more than 150°C in advance of slip casting. As an organic matter preferable to be used in the present invention is anyone selected from the group consisting of methyl carbonate, t-butyl alcohol, stearic acid, stearyl alcohol and paraffin.
  • A mixture having the above-mentioned organic matter and powders incapable of being extracted by supercritical fluid is formed into a compact, and the compact is used as a mold for slip casting. For the powders, metal powders and ceramic powders are preferable.
  • As the metal powders, powders of 1 to 1,000 µm in particle size having good flowability is preferable. For example, iron powders and iron alloy powders which are manufactured by means of gas atomizing method are preferable. As ceramic powders, powders of 0.2 to 10 µm in particle size having good flowability are preferable. For example, silica and alumina can be mentioned.
  • Futhermore, it is preferable that a mixture of an organic matter and powders consists of vol. 45% or less of the powders and the rest of the organic matter. The organic matter alone can be used in stead of the mixture. If the ratio of the powders is of 45wt.% or less, the mold breaks down of itself by means of extracting the organic matter supercritically. If the ratio is over 45wt.%, the mold gets hard to break down of itself. If the mixture is used, the amount of the organic matter can be decreased, compared with the case of the organic matter alone being used. So, time for extraction can be shortened. It is recommendable that the formation of the mixture or of the organic matter alone is performed by means of press forming or cast forming.
  • The mold of a compact having the organic matter and the powders incapable of being extracted by means of the supercritical fluid or the mold having exclusively the organic matter capable of being extracted by means of the supercritical fluid can be prepared by the following methods:
    • (1) The whole mold is composed of a formed compact of the present invention; or
    • (2) a part of the mold is composed of a formed compact of the present invention, and the rest of a formed compact having a feature of absorbing liquid or of not absorbing liquid, thereby those compacts being assembled into the mold. For the compact with the feature of absorbing liquid, gypsum or porous resin, and for the compact with the feature of not absorbing liquid, metal or rubber is used.
  • Metal powder or ceramic powder is dispersed into the liquid dispersion medium to prepare slurry, the liquid dispersion medium being water, organic solvent and paraffin. As the organic solvent, methyl carbonate, t-butyl alcohol, methyl alcohol, ethyl alcohol, butyl alcohol, hexane and benzene are preferable. Paraffin of 40 to 80°C can be preferably used. When water is used as the dispersion medium, ceramic oxide such as alumina and zirconium is dispersed. When the organic solvent is used, in addition to the ceramic oxide, non-oxide ceramics such as silicon nitride, silicon carbide and aluminium nitride are dispersed. When the paraffin is used, ceramic oxide and non-oxide ceramics are dispersed.
  • The slurry thus prepared is cast into the mold formed in the manner as mentioned in the above. After a part of the dispersion medium is absorbed in the mold, or the dispersion medium is solidified, separable parts constituting the mold are taken away. Parts hard to be separated constituting the mold i.e. a core of a complicated shape is formed by letting an organic matter capable of being extracted by supercritical fluid contained in the core. A compact is formed by means of slip casting, and then the compact is processed by a device for supercritical extraction, thereby the organic matter in the mold being removed and the mold being melted away or breaking down of itself.
  • If a dispersion medium contained in the compact is formed out of an organic matter capable of being extracted, it is advantageous that in the process of the supercritical extraction, the removal of the dispersion medium in the compact is simultaneously performed. For the organic matter, methyl carbonate, t-butyl alcohol, methyl alcohol, ethyl alcohol, butyl alcohol, hexane and benzene can be preferably used. When a dispersion medium is not formed out of an organic matter capable of being extracted supercritically, the removal of the dispersion medium is continuted by the supercritical extraction together in combination with operation of heating and decomposition.
  • When the mold of the present invention is used, the mold melts away or breaks down of itself. Consequently, a hollow compact requiring such a complicatedly shaped core as to fail to be drawn out of the mold can be easily used. Moreover, when a main mold is prepared in accordance with the present invention, the main mold is not required to have a divisible consitution, and resultantly, a compact with precision in demension can be obtained. Besides, a dispersion medium constituting slip is not necessarily limited to water, and therefore, non-aqueous dispersion medium can be applied to molding not only ceramic powders but also metal powders and non-oxide ceramic powers. Furthermore, if a dispersion medium in the compact is formed out of an organic matter capable of being extracted supercritically, the dispersion in the compact can be simultaneously removed.
  • Example-1
  • With specific reference to Figs. 1 to 3 of the drawings, an example of the present invention will now be described.
  • Granular paraffin having a melting point of 42 to 44°C was formed by hydraulic press into core 1 of a shape of a disc with a cylinder put thereon, the size of the disc being 30mm in diameter and 10mm in thickness and the size of the cylinder being 10mm in diameter and 10mm in height. Fig. 1 shows an elevatioanl view of a mold for slip casting. Core 1 was assembled together with upper metallic mold 2 having a cooling jacket divisible into two portions and lower disc-shaped metallic mold 3 having gate 4 in its center axis to form a metal mold for slip casting. It should be noted that the metal mold thus formed had an inside diameter of 60mm and an inside height of 20mm.
  • Secondly, slip of cilicon nitride, using, as a dispersion medium, paraffin with a melting point of 42 to 44°C contained in a composition shown in Table 1, was heated and fluidized. The fluidized slip was cast into the metal mold for slip casting, which had been water-cooled, and was kept at a pressure of 3kg/cm² for 2 minutes and a half. And then, the metal mold was demolded, and molded body 5 with core 1 attached thereto as shown in Fig. 2, was obtained. After cutting of the portion of gate 4 attached to molded body 5, the molded body was put into a device for supercritical extraction. In the device, using carbon dioxide as extraction solvent, the molded body was kept at 40°C and at 300kg/cm² for 2 hours, while carbon dioxide was passed therethrough to remove paraffin and oleic acid. Subsequently, the carbon dioxide was exhausted by two hour pressure reduction, and then, resultantly, as shown in Fig. 3, the core having disappeared and the dispersion medium having been extracted, finally molded body 6 was obtained.
    Figure imgb0001
  • Example-2
  • 71wt.% alumina was added to 29wt.% granular paraffin having a melting point of 42 to 44°C to prepare a mixture. The mixture was heated to 60°C to be in the state of melting and then it was stirred and mixed. Thereafter, the mixture was cast into the same metal mold as used in Example-1. The metal mold was cooled and demolded to obtain a similar core to that (core 1) shown in Fig. 1, and then, the same metallic mold for slip casting as used in Example-1 was constituted.
  • Subsequently, slip of silicon nitride, using paraffin used in Example-1 as a dispersion medium, was put into the casting operation, and followed by the supercritical extraction performance. Resultantly, a finally molded body from which the dispersion medium was removed and which retained the alumina in it, was obtained. The alumina remaining was such as can be easily extracted.

Claims (7)

  1. A mold for slip casting comprising a compact (I) formed of a mixture of organic matter and powders, characterized in that said organic matter is capable of being extracted by supercritical fluid and having a melting point of 0 to 150°C and said powders are incapable of being extracted by the supercritical fluid.
  2. The mold according to claim 1, characterized in that said organic matter is present in more than 55 and less than 100 vol.%.
  3. The mold according to claims 1 or 2, characterized in that said organic matter is selected from methyl carbonate, t-butyl alcohol, stearic acid, stearyl alcohol and paraffin.
  4. The mold according to claims 1, 2 or 3, characterized in that said powders are selected from metal powders and ceramic powders.
  5. The mold according to claims 1 to 4, characterized in that said compact (I) includes a core.
  6. A method for slip casting, characterized by using a compact (I) in a mold according to claims 1 to 5.
  7. Use of a compact (I) according to claims 1 to 5 in a mold for slip casting according to claims 1 to 5.
EP88107320A 1987-06-12 1988-05-06 Mold for slip casting Expired - Lifetime EP0294596B1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP62145326A JPS63309403A (en) 1987-06-12 1987-06-12 Mold for casting and molding of slurry
JP145326/87 1987-06-12

Publications (3)

Publication Number Publication Date
EP0294596A2 EP0294596A2 (en) 1988-12-14
EP0294596A3 EP0294596A3 (en) 1989-12-27
EP0294596B1 true EP0294596B1 (en) 1991-10-16

Family

ID=15382576

Family Applications (1)

Application Number Title Priority Date Filing Date
EP88107320A Expired - Lifetime EP0294596B1 (en) 1987-06-12 1988-05-06 Mold for slip casting

Country Status (4)

Country Link
US (1) US5035847A (en)
EP (1) EP0294596B1 (en)
JP (1) JPS63309403A (en)
DE (1) DE3865533D1 (en)

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0813446B2 (en) * 1990-05-30 1996-02-14 株式会社日立製作所 Slip casting method
JPH0557713A (en) * 1991-09-05 1993-03-09 Toyota Motor Corp Method for molding of fine pieces
IL109497A (en) * 1993-05-05 1998-02-22 Hyperion Catalysis Int Three-dimensional macroscopic assemblages of randomly oriented carbon fibrils and composites containing same
DE69511067T2 (en) 1994-01-31 1999-12-09 Bausch & Lomb METHOD FOR TREATING CONTACT LENSES WITH SUPERCRITICAL FLUIDUM
US5607518A (en) * 1995-02-22 1997-03-04 Ciba Geigy Corporation Methods of deblocking, extracting and cleaning polymeric articles with supercritical fluids
US5860467A (en) * 1996-12-03 1999-01-19 The University Of North Carolina At Chapel Hill Use of CO2 -soluble materials in making molds
US5996682A (en) * 1998-03-09 1999-12-07 General Motors Corporation Method of making a mold for metal casting

Family Cites Families (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE872C (en) * 1877-10-15 F. W. KOTTGEN in Barmen Peculiar arrangement of a twin Kalancir machine for lifting water
US1087974A (en) * 1910-04-01 1914-02-24 Herbert S Owen Manufacture of products of concrete, cement, and the like.
DE1533035B1 (en) * 1965-06-17 1971-04-01 Tavkoezlesi Ki PROCESS FOR POWDER METALLURGICAL PRODUCTION OF SINTER PARTS MADE OF METAL AND OR METAL OXIDE POWDER USING CAST PASTE
US4127629A (en) * 1976-07-28 1978-11-28 Norton Company Process of forming silicon carbide bodies
JPS59190811A (en) * 1983-04-15 1984-10-29 株式会社日立製作所 Mold for slip casting
US4604141A (en) * 1983-04-15 1986-08-05 Hitachi, Ltd. Slip casting mold
JPS61155265A (en) * 1984-12-26 1986-07-14 住友重機械工業株式会社 Removal of binder in formed body by supercritical fluid
JPS61155264A (en) * 1984-12-26 1986-07-14 住友重機械工業株式会社 Removal of binder in formed body by liquefied fluid
KR890003502B1 (en) * 1985-02-08 1989-09-23 가부시기가이샤 히다찌세이사꾸쇼 Method for shaping slip-casting and shaping moulds
JPS61261274A (en) * 1985-05-14 1986-11-19 日本鋼管株式会社 Method of forming powder

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
DE - B - C 3872 *

Also Published As

Publication number Publication date
JPH0420764B2 (en) 1992-04-06
EP0294596A3 (en) 1989-12-27
US5035847A (en) 1991-07-30
JPS63309403A (en) 1988-12-16
DE3865533D1 (en) 1991-11-21
EP0294596A2 (en) 1988-12-14

Similar Documents

Publication Publication Date Title
EP0206685B1 (en) Method for molding a pulverulent material
EP0255577A1 (en) Method of producing mold for slip casting
US4989664A (en) Core molding composition
JPS6045973B2 (en) Normal solidification casting method for superalloys
BE1010959A3 (en) METHOD FOR MANUFACTURING EXOTHERMIC SLEEVES AND CASTING OF METAL PARTS, AND SLEEVES AND METAL PARTS OBTAINED THEREBY.
EP0294596B1 (en) Mold for slip casting
US5468285A (en) Ceramic core for investment casting and method for preparation of the same
JPH0319802A (en) Making of ceramic mold by freezing of water slip
JPH0824996B2 (en) Water-soluble core and method for producing the same
GB2163780A (en) Method of moulding powder materials
JPH0270007A (en) Method for casting and molding powder
JPH0436117B2 (en)
EP0240190B1 (en) Process for manufacturing ceramic sintered bodies and mold to be used therefor
KR100493950B1 (en) Method for making High Density Stainless Steel Sintering Material
EP0140682A1 (en) A method for producing a ceramic article
JP4889306B2 (en) Silicone coagulation mold with mold release material
JPH0753803Y2 (en) Spout bush
JPH0892605A (en) Core for injection-molding sintered article and production of sintered article using the core
JP2934220B2 (en) Semi-solid and semi-solid casting
EP0233478A1 (en) Mold, method of producing mold and casting method
EP0294597A2 (en) Method of manufacturing a sintered body of silicon nitride
JPH05200711A (en) Method for molding powder
FR2845988A1 (en) Ceramic mixture with a refractory plaster base and charged with minerals to improve the strength of the refractory blocks used in precision casting operations for a wide range of industries
KR100493949B1 (en) Binder for high density stainless steel sintering material and method for making high density stainless steel sintering material using the same
JPS63264259A (en) Sand core for pressure casting

Legal Events

Date Code Title Description
PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

17P Request for examination filed

Effective date: 19880506

AK Designated contracting states

Kind code of ref document: A2

Designated state(s): DE FR GB SE

PUAL Search report despatched

Free format text: ORIGINAL CODE: 0009013

AK Designated contracting states

Kind code of ref document: A3

Designated state(s): DE FR GB SE

17Q First examination report despatched

Effective date: 19900817

GRAA (expected) grant

Free format text: ORIGINAL CODE: 0009210

AK Designated contracting states

Kind code of ref document: B1

Designated state(s): DE FR GB SE

REF Corresponds to:

Ref document number: 3865533

Country of ref document: DE

Date of ref document: 19911121

ET Fr: translation filed
PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: GB

Payment date: 19920429

Year of fee payment: 5

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: FR

Payment date: 19920430

Year of fee payment: 5

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: SE

Payment date: 19920518

Year of fee payment: 5

PLBE No opposition filed within time limit

Free format text: ORIGINAL CODE: 0009261

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: NO OPPOSITION FILED WITHIN TIME LIMIT

26N No opposition filed
PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: GB

Effective date: 19930506

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: SE

Effective date: 19930507

GBPC Gb: european patent ceased through non-payment of renewal fee

Effective date: 19930506

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: FR

Effective date: 19940131

REG Reference to a national code

Ref country code: FR

Ref legal event code: ST

EUG Se: european patent has lapsed

Ref document number: 88107320.9

Effective date: 19931210

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: DE

Payment date: 19950511

Year of fee payment: 8

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: DE

Effective date: 19970201